Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/67—Unsaturated compounds having active hydrogen
  • C08G18/671—Unsaturated compounds having only one group containing active hydrogen
  • C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
  • C08F290/06—Polymers provided for in subclass C08G
  • C08F290/067—Polyurethanes; Polyureas
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/16—Catalysts
  • C08G18/22—Catalysts containing metal compounds
  • C08G18/227—Catalysts containing metal compounds of antimony, bismuth or arsenic
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/48—Polyethers
  • C08G18/4825—Polyethers containing two hydroxy groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/72—Polyisocyanates or polyisothiocyanates
  • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
  • C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
  • C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/72—Polyisocyanates or polyisothiocyanates
  • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
  • C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
  • C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
  • C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
  • C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
  • C08L75/04—Polyurethanes
  • C08L75/14—Polyurethanes having carbon-to-carbon unsaturated bonds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
  • C08L75/04—Polyurethanes
  • C08L75/14—Polyurethanes having carbon-to-carbon unsaturated bonds
  • C08L75/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
  • C09J175/04—Polyurethanes
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
  • C09J175/04—Polyurethanes
  • C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
  • C09J175/04—Polyurethanes
  • C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
  • C09J175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds

Definitions

• the present invention relates to a composition based on a methacrylate monomer.
• the invention also relates to the use of said composition for the repair and / or the semi-structural or structural bonding of materials in the field of transport, marine, assembly or construction.
• Acrylic compositions are known reactive systems crosslinking by radical polymerization. They are used as adhesives, sealants and coatings. Radical polymerization is typically initiated by a redox system which through an oxidation-reduction reaction results in the production of radicals.
• the majority of acrylic systems are two-component systems.
• the first component traditionally contains the reducing agent and reactive monomers, and the second component contains the oxidizing agent. Once the two components are mixed, the reducing agent induces the cleavage of the 0-0 bond of organic peroxide, for example, and initiates polymerization.
• Acrylates and methacrylates, especially those with alkyl radicals, are monomers exhibiting a high vapor pressure. This has the consequence that they are odorous when applied.
• the hydroxyl number of an alcoholic compound represents the number of hydroxyl functions per gram of product, which is expressed in the form of the equivalent number of milligrams of potash (mg KOH / g) used in the determination of the hydroxyl functions, per gram of product;
• the viscosity measurement at 23 ° C can be done using a Brookfield viscometer according to the ISO 2555 standard.
• the measurement carried out at 23 ° C (or at 100 ° C) can be done using a Brookfield RVT viscometer, a needle adapted to the viscosity range and at a rotational speed of 20 revolutions per minute (rev / min);
• the present invention also relates to a two-component composition
• a two-component composition comprising:
• component A comprising:
• M1 (meth) acrylate monomer chosen from the following compounds and their mixtures:
• component B comprising:
• the polyurethane P can have a number-average molecular mass (Mn) greater than or equal to 2,000 g / mol, preferably greater than or equal to 5,000 g / mol, preferably greater than or equal to 7,000 g / mol, better still greater or equal to 10,000 g / mol.
• Mn number-average molecular mass
• Polyurethane P can be obtained by a process comprising:
• step E2 the reaction of the product formed at the end of step E1) with at least one (meth) acrylate M2 monomer comprising at least one hydroxyl function.
• the usable polyisocyanate (s) can be added sequentially or reacted as a mixture.
• the polyisocyanate (s) can be chosen from diisocyanates or triisocyanates.
• the polyisocyanate (s) can be monomer (s), oligometic (s) or polymer (s).
• the polyisocyanate (s) are diisocyanate (s), preferably chosen from the group consisting of isophorone diisocyanate (I PDI), hexamethylene diisocyanate (HDI), heptane diisocyanate, octane diisocyanate, nonane diisocyanate, decane diisocyanate, undecane diisocyanate, dodecane diisocyanate, 2,4'-methylenebis (cyclohexylisocyanate) (2,4'-H6MDI), 4,4'- methylenebis (cyclohexylisocyanate) (4,4'-H6MDI), norbornane diisocyanate, norbornene diisocyanate,
• R c represents a hydrocarbon chain, saturated or unsaturated, cyclic or acyclic, linear or branched, comprising from 1 to 20 carbon atoms, preferably from 6 to 14 carbon atoms
• R d represents a divalent alkylene group, linear or branched, having from 2 to 4 carbon atoms, and preferably a divalent propylene group; and their mixtures.
• the allophanate of formula (Y) above is such that p, q, R c and R d are chosen such that the HDI allophanate derivative above comprises an isocyanate group NCO content ranging from 12 to 14 % by weight relative to the weight of said derivative.
• the polyisocyanate (s) which can be used are triisocyanate (s), preferably chosen from isocyanurates, biurets, and adducts of diisocyanates and triols.
• the isocyanurate (s) can be used (s) in the form of a technical mixture of (poly) isocyanurate (s) with a purity of greater than or equal to 70% by weight isocyanurate (s).
• the diisocyanate isocyanurate (s) which can be used according to the invention can (wind) correspond to the following general formula (W):
• R 5 represents an alkylene group, linear or branched, cyclic, aliphatic, arylaliphatic or aromatic, comprising from 4 to 9 carbon atoms, with the proviso that the NCO groups are not linked by a covalent bond to a carbon atom forming part of an aromatic hydrocarbon ring such as a phenyl group.
• trimers of diisocyanates which can be used according to the invention, there may be mentioned:
• HDI hexamethylene diisocyanate
• the polyisocyanate (s) is (are) chosen from diisocyanates, preferentially from toluene diisocyanate (in particular the 2,4 TDI isomer, the 2,6-TDI isomer or their mixtures. ), 4,4'-diphenylmethanediisocyanate, 2,4'-diphenylmethane diisocyanate, meta-xylylene diisocyanate (m-XDI), isophorone diisocyanate (IPDI), and mixtures thereof.
• diisocyanates preferentially from toluene diisocyanate (in particular the 2,4 TDI isomer, the 2,6-TDI isomer or their mixtures. ), 4,4'-diphenylmethanediisocyanate, 2,4'-diphenylmethane diisocyanate, meta-xylylene diisocyanate (m-XDI), isophorone diisocyanate (IPDI), and
• the polyisocyanate is chosen from polyisocyanates based on diphenylmethane diisocyanate (MDI), and in particular from monomeric and polymeric polyisocyanates.
• MDI diphenylmethane diisocyanate
• Diphenylmethane diisocyanate may be in the form of a single isomer, for example chosen from 2,4'-MDI and 4,4'-MDI, or in the form of a mixture of isomers, for example 2, 4 '-MDI and 4,4'-MDI.
• the polyisocyanate (s) which can be used is (are) typically available commercially.
• SCURANATE® TX marketed by the company VENCOREX, corresponding to a 2,4-TDI with a purity of the order of 95%
• SCURANATE® T100 marketed by the company VENCOREX
• the “DESMODUR® I” marketed by the company COVESTRO
• corresponding to an isocyanurate of HDI the “TAKENATE TM 500” marketed by MITSUI CHEMICALS corresponding to an m-XDI
• TAKENATE TM 600 marketed by MITSUI CHEMICALS corresponding to an m-H6XDI
• the “VESTANAT® H12MDI” marketed by EVONIK
• the polyisocyanate is chosen from:
• Monomeric diphenylmethane diisocyanate such as, for example, a mixture of approximately 70% by weight of 4,4′-MDI monomer and 30% by weight of 2,4′-MDI monomer, or 4,4′-MDI; or the 4,4'-MDI alone;
• the polyol (s) can be chosen from polyester polyols, polyether polyols, polyene polyols, polycarbonate polyols, poly (ether-carbonate) polyols, and mixtures thereof.
• the polyol (s) which can be used can be chosen from aromatic polyols, aliphatic polyols, arylaliphatic polyols and mixtures of these compounds.
• the polyol (s) which can be used can be chosen from among those having a number-average molecular weight (Mn) ranging from 200 g / mol to 20,000 g / mol, preferably from 400 g / mol to 18,000 g / mol.
• Mn number-average molecular weight
• the number-average molecular weight of the polyols can be calculated from the hydroxyl number (IOH) expressed in mg KOH / g and the functionality of the polyol or determined by methods well known to those skilled in the art, by example by steric exclusion chromatography (or SEC in English) with standard PEG (polyethylene glycol).
• the polyols have a hydroxyl functionality ranging from 2 to 6.
• the hydroxyl functionality of a polyol is the average number of hydroxyl functions per mole of polyol.
• the polyester polyol (s) may have a number average molecular weight ranging from 1000 g / mol to 10,000 g / mol, preferably from 2000 g / mol to 6000 g / mol. .
• polyester polyols mention may for example be made of:
• polyester polyols of natural origin such as castor oil
• aliphatic (linear, branched or cyclic) or aromatic polyols such as for example monoethylene glycol, diethylene glycol, 1, 2-propanediol, 1, 3-propanediol, 1, 4-butanediol, butenediol, 1,6-hexanediol, cyclohexane dimethanol, tricyclodecane dimethanol, neopentyl glycol, cyclohexane dimethanol, a polyether polyol, glycerol, trimethylolpropane, 1, 2,6-hexanetriol, sucrose, glucose , sorbitol, pentaerythritol, mannitol, N-methyldiethanolamine, triethanolamine, a dimeric fatty alcohol, a trimeric fatty alcohol, and mixtures thereof, with
• polycarboxylic acid or its ester or anhydride derivative such as 1, 6-hexanedioic acid (adipic acid), dodecanedioic acid, azelaic acid, sebacic acid, adipic acid, acid 1, 18-octadecanedioic acid, phthalic acid, isophthalic acid, terephthalic acid, succinic acid, a dimeric fatty acid, a trimeric fatty acid and mixtures of these acids, an unsaturated anhydride such as for example l maleic or phthalic anhydride, or a lactone such as, for example, caprolactone;
• an unsaturated anhydride such as for example l maleic or phthalic anhydride
• a lactone such as, for example, caprolactone
• polyester polyols can be prepared in a conventional manner, and for the most part are commercially available.
• polyester polyols mention may for example be made of the following products with a hydroxyl functionality equal to 2:
• TONE® 0240 (marketed by UNION CARBIDE) which is a polycaprolactone with a number-average molecular mass of approximately 2000 g / mol, and a melting point of approximately 50 ° C,
• DYNACOLL® 7360 (marketed by EVONIK) which results from the condensation of adipic acid with hexanediol, and has a number-average molecular mass of approximately 3500 g / mol, and a melting point of 55 Approx. ° C,
• polyester polyol having a viscosity of 180 Pa.s at 23 ° C, a number-average molecular mass Mn equal to 5500 g / mol, and a T g equal to - 50 ° C,
• KURARAY® P-6010 polyester polyol having a viscosity of 68 Pa.s at 23 ° C, a number-average molecular mass Mn equal to 6000 g / mol, and a T g equal at -64 ° C,
• KURARAY® P-10010 polyester polyol having a viscosity of 687 Pa.s at 23 ° C, and a number-average molecular mass Mn equal to 10,000 g / mol
• polyester polyol having a number-average molecular mass Mn close to 1000 g / mol and whose hydroxyl number ranges from 108 to 116 mg KOH / g. It is a product resulting from the condensation of adipic acid, diethylene glycol and monoethylene glycol,
• DEKATOL® 3008 (marketed by the company BOSTIK) with a number-average molar mass Mn close to 1060 g / mol and whose hydroxyl number ranges from 102 to 112 mg KOH / g. It is a product resulting from the condensation of adipic acid, diethylene glycol and monoethylene glycol; - “PRIPLAST® 3186” (marketed by CRODA): bio-based polyester polyol having an IHO equal to 66 mg KOH / g;
• the polyether polyol (s) can have a number-average molecular mass ranging from 200 to 20,000 g / mol, preferably from 300 to 12,000 g / mol, and preferably from 400 at 4000 g / mol.
• the polyether polyol (s) which can be used according to the invention is (are) preferably chosen from polyoxyalkylene polyols, in which the alkylene part, linear or branched, comprises from 1 to 4 carbon atoms, more preferably from 2 to 3 carbon atoms.
• the polyether polyol (s) which can be used according to the invention is (are) preferably chosen from polyoxyalkylene diols or polyoxyalkylene triols, of which the alkylene part, linear or branched, comprises 1 with 4 carbon atoms, more preferably from 2 to 3 carbon atoms.
• Polyoxypropylene diols or triols also referred to as polypropylene glycol (PPG) diols or triols
• PPG polypropylene glycol
• Mn number average molecular mass
• polyoxyethylene diols or triols also designated by polyethylene glycol (PEG) diols or triols
• Mn number-average molecular mass
• polyether polyols can be prepared in a conventional manner, and are widely available commercially. They can be obtained by polymerization of the corresponding alkylene oxide in the presence of a basic catalyst (for example potassium hydroxide) or of a catalyst based on a double metal-cyanide complex.
• a basic catalyst for example potassium hydroxide
• a catalyst based on a double metal-cyanide complex for example sodium bicarbonate
• VORANOL® P1010 sold by the company DOW with a number-average molecular mass (Mn) of around 1020 g / mol and whose hydroxyl number is around 110 mg KOH / g;
• VORANOL® P2000 sold by the company DOW, a difunctional PPG with a number-average molecular mass of approximately 2000 g / mol
• - VORANOL® EP 1900 sold by the company DOW, a difunctional PPG with a number-average molecular mass of approximately 4,008 g / mol, and of hydroxyl number lo H equal to 28 mg KOH / g;
• - ACCLAIM ® 4200 difunctional PPG with a number-average molecular mass of approximately 4000 g / mol, and a hydroxyl number lo H equal to 28 mg KOH / g;
• - ACCLAIM ® 8200 difunctional PPG with a number-average molecular mass of 8,016 g / mol, and a hydroxyl number lo H equal to 14 mg KOH / g;
• - ACCLAIM ® 12200 difunctional PPG with a number-average molecular mass of 11222 g / mol, and a hydroxyl number lo H equal to 10 mg KOH / g;
• - ACCLAIM ® 18200 difunctional PPG with a number-average molecular mass of 17,265 g / mol, and a hydroxyl number lo H equal to 6.5 mg KOH / g.
• polyether triol By way of example of polyether triol, mention may be made of the polyoxypropylene triol marketed under the name “VORANOL® CP 450” by the company DOW, with a number-average molecular mass (Mn) close to 450 g / mol and whose index hydroxyl ranges from 370 to 396 mg KOH / g, or the polyoxypropylene triol marketed under the name “VORANOL® CP3355” by the company DOW, with a number-average molecular mass close to 3,554 g / mol, or “ACCLAIM® 6300 Which is a trifunctional PPG with a number-average molecular mass of approximately 5,948 g / mol, and of hydroxyl number lo H equal to 28.3 mg KOH / g.
• Mn number-average molecular mass
• ACCLAIM® 6300 which is a trifunctional PPG with a number-average molecular mass of approximately 5,948 g / mol
• the polyene polyol (s) which can be used according to the invention can be preferably chosen from polyenes comprising terminal hydroxyl groups, and their corresponding hydrogenated or epoxidized derivatives.
• the polyene polyol (s) which can be used according to the invention is (are) chosen from polybutadienes comprising terminal hydroxyl groups, optionally hydrogenated or epoxidized.
• the polyene polyol (s) which can be used according to the invention is (are) chosen from homopolymers and copolymers of butadiene comprising terminal hydroxyl groups, optionally hydrogenated or epoxidized.
• terminal hydroxyl groups of a polyene polyol is understood to mean the hydroxyl groups located at the ends of the main chain of the polyene polyol.
• the hydrogenated derivatives mentioned above can be obtained by total or partial hydrogenation of the double bonds of a polydiene comprising terminal hydroxyl groups, and are therefore saturated or unsaturated.
• the epoxidized derivatives mentioned above can be obtained by chemioselective epoxidation of the double bonds of the main chain of a polyene comprising terminal hydroxyl groups, and therefore comprise at least one epoxy group in its main chain.
• polyene polyols mention may be made of the homopolymers of butadiene, saturated or unsaturated, comprising terminal hydroxyl groups, optionally epoxidized, such as, for example, those sold under the name “POLY BD® or KRASOL®” by the company.
• CRAY VALLEY as well as isoprene homopolymers, saturated or unsaturated, comprising terminal hydroxyl groups, such as, for example, those sold under the name “POLY IP TM or EPOL TM” by the company IDEMITSU KOSAN.
• the polycarbonate polyols can be chosen from polycarbonate diols or triols, having in particular a number-average molecular weight (M n ) ranging from 300 to 12,000 g / mol.
• polycarbonate diol By way of example of polycarbonate diol, mention may be made of: “CONVERGE® POLYOL 212-10” and “CONVERGE® POLYOL 212-20” marketed by the company NOVOMER, respectively with a molecular mass in number (M n ) equal to 1000 and 2000 g / mol, the hydroxyl numbers of which are respectively 1 12 and 56 mg KOH / g, the “DESMOPHEN® C XP 2716” marketed by COVESTRO with a number molecular mass (M n ) equal to 326 g / mol and of which the hydroxyl number is 344 mg KOH / g, the “POLYOL C-590, C1090, C-2090 and C-3090” marketed by KURARAY having a number molecular mass (M n ) ranging from 500 to 3,000 g / mol and a hydroxyl number ranging from 224 to 37 mg KOH / g.
• M n mo
• the (meth) acrylate monomer M2 can be chosen from those having the following formula (I): [Chem 10]
• - R 6 represents a methyl or a hydrogen, preferably R 6 being a methyl;
• the M2 monomer has one of the following formulas: - Formula (1-1):
• R 7 represents a divalent linear or branched alkylene radical, aliphatic or cyclic, saturated or unsaturated, comprising from 2 to 22 carbon atoms, preferably from 2 to 18, preferably from 2 to 14, even more preferably from 2 to 10, and advantageously from 2 to 6 carbon atoms;
• - w is an integer ranging from 1 to 10, preferably from 1 to 5, and preferably w is equal to 5;
• - s is an integer ranging from 1 to 10, s preferably being equal to 2;
• R 8 represents a divalent linear or branched alkylene radical, aliphatic or cyclic, saturated or unsaturated, comprising from 2 to 22 carbon atoms, preferably from 2 to 18, preferably from 2 to 14, even more preferably from 2 to 10, and advantageously from 2 to 6 carbon atoms;
• R 9 represents a divalent linear or branched alkylene radical, aliphatic or cyclic, saturated or unsaturated, comprising from 2 to 4 carbon atoms, t is an integer ranging from 2 to 120, preferably from 1 to 10, t being from preferably equal to 2 or 3.
• HEMA 2-hydroxyethyl methacrylate
• HPA 2-hydroxypropyl methacrylate
• 4-hydroxybutyl acrylate 2-hydroxybutyl methacrylate
• HPA 2-hydroxypropyl acrylate
• SARTOMER COGNIS or BASF
• the M2 monomer is 2-hydroxyethyl methacrylate (HEMA):
• Step E1) The polyaddition reaction E1) can be carried out at a temperature preferably below 95 ° C. and / or under conditions which are preferably anhydrous.
• the polyaddition reaction can be carried out in the presence or absence of at least one catalyst.
• the reaction catalyst (s) which can be used during the polyaddition reaction can be any catalyst known to those skilled in the art for catalyzing the formation of polyurethane by reaction of at least one polyisocyanate with at least one polyol.
• An amount of up to 0.3% by weight of catalyst (s) relative to the weight of the reaction medium of the polyaddition step can be used.
• the polyaddition reaction E1) can be carried out in the presence or absence of at least one solvent.
• the solvent can be chosen from solvents which do not react with the reactive functions of the ingredients used in step E1). It can, for example, be methyl methacrylate, toluene, ethyl acetate, xylene, and mixtures thereof.
• Step E1) is preferably carried out in amounts of reagents such that the NCO / OH (r1) molar ratio ranges from 1.5 to 5, preferably from 1.5 to 2.5.
• (r1) is the NCO / OH molar ratio corresponding to the molar ratio of the number of isocyanate groups (NCO) to the number of hydroxyl groups (OH) carried by respectively by the all of the polyisocyanate (s) and all of the alcohol (s) present in the reaction medium of step E1) (polyol (s)).
• the polyurethane obtained in step E1) preferably has two NCO groups at the terminal position of the main chain.
• Step E2) can be carried out at a temperature preferably below 80 ° C, preferably below or equal to 60 ° C, and / or under preferably anhydrous conditions.
• Step E2) can be carried out in the presence or absence of at least one catalyst. It can be the same catalyst as that used in step E1).
• Step E2) can be carried out in the presence or absence of at least one solvent.
• the solvent can be chosen from solvents which do not react with the reactive functions of the ingredients used in step E2). It can, for example, be methyl methacrylate, toluene, ethyl acetate, xylene, and mixtures thereof.
• step E2) is carried out by adding the monomer (s) M2 to the reaction medium of step E1), without isolation of the product formed in step E1).
• Step E2) is preferably carried out in quantities of reagents such that the OH / NCO (r2) molar ratio is less than or equal to 1, preferably ranges from 0.90 to 1.00, and even more preferably ranges from 0.95 to 1.00.
• (r2) is the OH / NCO molar ratio corresponding to the molar ratio of the number of hydroxyl groups (OH) to the number of isocyanate groups (NCO) carried respectively by the assembly alcohol (s), and isocyanate (s) (especially polyurethane with NCO terminations and optionally unreacted polyisocyanate (s) at the end of step E1) ) present in the reaction medium of step E2).
• the polyurethane P can be in solution in a solvent such as, for example, methyl methacrylate.
• the polyurethane content in the solution can range from 40% to 80% by weight, preferably from 50% to 70% by weight.
• the total content of polyurethane P in component A may be greater than or equal to 5% by weight, preferably greater than or equal to 8% by weight, even more preferably greater than or equal to 10% by weight, and advantageously greater than or equal to 13% by weight, based on the total weight of component A.
• the monomer M1 is chosen from the following compounds and their mixtures: [Chem 15]
• the (meth) acrylate monomer M1 is a methacrylate monomer.
• component A comprises a mixture of the following compounds: [Chem 16]
• the total content of M1 (meth) acrylate monomer (s) in component A may be greater than or equal to 30% by weight, preferably greater than or equal to 40% by weight, even more preferably greater than or equal to 50% by weight , and in particular greater than or equal to 55% by weight relative to the total weight of component A.
• the reducing agent can be chosen from tertiary amines, sodium metabisulfite, sodium bisulfite, transition metals, azo compounds, alpha-aminosulfones, and mixtures thereof.
• the reducing agent can be contained in the polyurethane P.
• This embodiment is for example possible when in step E1) above-mentioned, the polyols and the polyisocyanates are reacted with a tertiary amine having pendant hydroxyl functions such as by example bisomer® PTE marketed by GEO SPECIALITY CHEMICALS or else N- (2-hydroxyethyl) -N-methyl aniline or even N- (2-hydroxyethyl) -N-methyl-p-toluidine.
• a tertiary amine having pendant hydroxyl functions such as by example bisomer® PTE marketed by GEO SPECIALITY CHEMICALS or else N- (2-hydroxyethyl) -N-methyl aniline or even N- (2-hydroxyethyl) -N-methyl-p-toluidine.
• azo compounds mention may for example be made of azoisobutyric acid.
• alpha-sulfones mention may for example be made of bis (tolylsulfonmethyl) benzylamine.
• DIIPT diisopropanol-p-toluidine
• dimethyl-p-toluidine dipropoxy-p-toluidine
• dimethylaniline N, N-dimethylaminomethylphenol
• N, N-diisopropanol-p-chloroaniline N, N-diisopropanol-p-bromoaniline
• N N-dimethyl-p-chloroaniline
• N-dimethyl-p-bromoaniline N, N-diethyl-p-chloroaniline
• N, N-diethyl-p-bromoaniline N, N-diethyl-p-bromoaniline; and their mixtures.
• component A comprises at least one tertiary amine.
• Component A may comprise a reducing agent content ranging from 0.5% to 5%, preferably from 0.5% to 3%, by weight relative to the total weight of component A
• the oxidizing agent can be chosen from peroxides, organic salts of transition metals, compounds containing labile chlorine, and mixtures thereof.
• the peroxide can be chosen from organic peroxides, inorganic peroxides, and mixtures thereof.
• peroxydisulfuric acid and their salts such as ammonium peroxodisulfate, sodium peroxodisulfate and potassium peroxodisulfate.
• organic peroxides mention may be made of cumene hydroperoxide, para-menthane hydroperoxide, tert-butyl peroxyisobutyrate, tert-butyl peroxybenzoate, tert-butyl peroxyneodecanoate, tert-amyl peroxypivalate, acetyl peroxide, benzoyl peroxide, dibenzoyl peroxide, 1,3-bis- (t-butylperoxyisopropyl) benzene, diacetyl peroxide, t-butylcumyl peroxide, tert-butyl peroxyacetate, cumyl, 2,5-dimethyl-2,5-di-t-butylperoxyhexane, 2,5-dimethyl-2,5-di-t-butyl-peroxyhex-3-yne, 4-methyl-2,2 -di-t-butylperoxypentane, and mixture
• component B comprises benzoyl peroxide
• Component B may comprise a total content of reducing agent greater than or equal to 20% by weight, preferably greater than or equal to 30% by weight, advantageously greater than or equal to 50% by weight relative to the total weight of component B.
• the composition according to the invention can typically comprise a redox system, a reducing agent being included in part A and an oxidizing agent being included in part B.
• the following combinations can be mentioned, for example: persulphates (oxidant) / (sodium metabisulphite and / or sodium bisulfite) (reducing agents); organic peroxides (oxidizer) / tertiary amines (reducing agent); organic hydroperoxides (oxidant) / transition metals (reducing agent).
• the composition can include at least one (meth) acrylate monomer in component A and / or component B.
• the (meth) acrylate monomers can comprise one (monofunctional) or more (meth) acrylate (polyfunctional) functions.
• the (meth) acrylate monomer (s) can be chosen from the group consisting of:
• R 10 represents a hydrogen atom or an alkyl group comprising from 1 to 4 carbon atoms
• R 11 is chosen from the group consisting of alkyls, cycloalkyls, alkenyls, cycloalkenyls, alkylaryl, arylalkyl or aryl, said alkyls, cycloalkyl, alkenyl, cycloalkenyl, alkylaryl, arylalkyl or aryl which may be optionally substituted and / or interrupted by at least one silane, a silicone, an oxygen, a halogen, a carbonyl, a hydroxyl, an ester, a urea, a urethane, a carbonate, an amine, an amide, a sulfur, a sulfonate, or a sulfone;
• the (meth) acrylate monomer is chosen from methyl (meth) acrylate, ethyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, heptyl (meth) acrylate , 2-tert-butylheptyl (meth) acrylate, octyl (meth) acrylate, 3-isopropylheptyl (meth) acrylate, nonyl (meth) acrylate, decyl (meth) acrylate, ( undecyl meth) acrylate, 5-methylundecyl (meth) acrylate, dodecyl (meth) acrylate, 2-methyldodecyl (meth) acrylate, tridecyl (meth) acrylate, 5 (meth) acrylate -methyltridecyl, tetradecyl (meth) acrylate, pentadecyl (
• the (meth) acrylate monomer is a methacrylate.
• the (meth) acrylate monomer is methyl methacrylate.
• the composition does not comprise a (meth) acrylate monomer (apart from the monomer M1 specific for component A).
• the two-component composition according to the invention can comprise at least one additive chosen from the group consisting of catalysts, fillers, antioxidants, light stabilizers / UV absorbers, metal deactivators, antistatic agents, anti-fog agents, foaming agents, biocides, plasticizers, lubricants, emulsifiers, colorants, pigments, rheological agents, impact modifiers, adhesion promoters, optical brighteners, flame retardants, anti-seepage agents , nucleating agents, solvents, and mixtures thereof.
• additives chosen from the group consisting of catalysts, fillers, antioxidants, light stabilizers / UV absorbers, metal deactivators, antistatic agents, anti-fog agents, foaming agents, biocides, plasticizers, lubricants, emulsifiers, colorants, pigments, rheological agents, impact modifiers, adhesion promoters, optical brighteners, flame retardants, anti-seepage agents , nucleating agents, solvents, and mixtures
• additives may be present in component A and / or component B of the composition according to the invention.
• soybean oil such as, for example, sold under the name VIKOFLEX® 7170 by the company ARKEMA.
• rheological agent (s) which can be used, there may be mentioned any rheological agent usually used in the field of adhesive compositions.
• thixotropic agents are chosen from:
• - micronized amide waxes such as CRAYVALLAC SLX marketed by ARKEMA.
• composition according to the invention can further comprise at least one organic and / or mineral filler.
• the usable mineral filler (s) is (are) advantageously chosen so as to improve the mechanical performance of the composition according to the invention in the crosslinked state.
• mineral filler As an example of usable mineral filler (s), it is possible to use any mineral filler (s) usually used in the field of adhesive compositions. These fillers are typically in the form of particles of various geometry. They may for example be spherical, fibrous, or have an irregular shape.
• the filler (s) is (are) chosen from the group consisting of clay, quartz, carbonate fillers, kaolin, gypsum, clays, and their mixtures, preferably the filler (s) is (are) chosen from carbonate fillers, such as carbonates of alkali or alkaline earth metals, and more preferably calcium carbonate or chalk.
• These fillers can be untreated or treated, for example using an organic acid such as stearic acid, or a mixture of organic acids consisting mainly of stearic acid.
• composition according to the invention can also comprise at least one adhesion promoter, preferably chosen from silanes, such as aminosilanes, epoxysilanes or acryloylsilanes, or adhesion promoters based on phosphate ester.
• adhesion promoter preferably chosen from silanes, such as aminosilanes, epoxysilanes or acryloylsilanes, or adhesion promoters based on phosphate ester.
• 2-hydroxyethyl phosphate ester of methacrylate 2-methacryloyloxyethyl phosphate, bis- (2-methacryloyloxyethyl phosphate), 2-acryloyloxyethyl phosphate, bis- (2-acryloyloxyethyl phosphate), methyl- ( 2-methacryloyloxyethyl phosphate), ethyl- (2-methacryloyloxyethyl phosphate), a mixture of mono and di-phosphate esters of 2-hydroxyethyl methacrylate.
• a solvent in particular a volatile solvent
• its content is preferably less than or equal to 5% by weight, more preferably less than or equal to 3% by weight, relative to the total weight of the mixture. composition.
• the content of solvent (s) in the composition is between 0% and 5% by weight.
• a pigment When a pigment is present in the composition, its content is preferably less than or equal to 3% by weight, more preferably less than or equal to 2% by weight, relative to the total weight of the composition. When it is present, the pigment may for example represent from 0.1% to 3% by weight or from 0.4% to 2% by weight of the total weight of the composition.
• the pigments can be organic or inorganic pigments.
• the pigment is PO2, in particular KRONOS® 2059 sold by the company KRONOS.
• the composition may comprise an amount of 0.1% to 3%, preferably 1% to 3% by weight, of at least one UV stabilizer or antioxidant.
• UV stabilizer or antioxidant typically introduced to protect the composition from degradation resulting from a reaction with oxygen which may be formed by the action of heat or light.
• These compounds can include primary antioxidants which scavenge free radicals. Primary antioxidants can be used alone or in combination with other secondary antioxidants or UV stabilizers.
• IRGANOX® 1010 Mention may be made, for example, of IRGANOX® 1010, IRGANOX® B561, IRGANOX® 245, IRGAFOS® 168, TINUVIN® 328 or TINUVIN TM 770 sold by BASF.
• the component A / component B volume ratio in the composition of the invention ranges from 100/5 to 1/1, preferably from 20/1 to 1/1, preferably from 10/1 to 1 / 1.
• the aforementioned composition comprises:
• component A comprising:
• component B comprising:
• the composition according to the invention is an adhesive composition.
• the present invention also relates to a ready-to-use kit, comprising component A as defined above on the one hand and component B as defined above on the other hand, packaged in two separate compartments. It may for example be a two-component cartridge.
• composition according to the invention can be in a two-component form, for example in a ready-to-use kit, comprising component A on the one hand in a first compartment or barrel and component B d. 'on the other hand in a second compartment or barrel, in proportions suitable for direct mixing of the two components, for example using a metering pump.
• the kit further comprises one or more means allowing the mixing of components A and B.
• the mixing means are chosen from metering pumps, static mixers of diameter adapted to the quantities. used. Uses of compositions
• the present invention also relates to the use of a composition as defined above, as an adhesive, mastic or coating, preferably as an adhesive.
• the invention also relates to the use of said composition for the repair and / or the structural or semi-structural bonding of materials in the field of transport, automobile (car, bus or truck), assembly, marine, etc. or construction.
• the present invention also relates to a method of assembling two substrates by bonding, comprising:
• the crosslinking step can be carried out at a temperature between 0 ° C and 200 ° C, preferably between 10 ° C and 150 ° C, preferably between 23 and 80 ° C and in particular between 20 ° C and 25 ° C.
• Crosslinking can also be induced using microwaves.
• Suitable substrates are, for example, inorganic substrates such as concrete, metals or alloys (such as aluminum alloys, steel, non-ferrous metals and galvanized metals); or organic substrates such as wood, plastics such as PVC, polycarbonate, PMMA, polyethylene, polypropylene, polyesters, epoxy resins; metal substrates and painted composites.
• inorganic substrates such as concrete, metals or alloys (such as aluminum alloys, steel, non-ferrous metals and galvanized metals); or organic substrates such as wood, plastics such as PVC, polycarbonate, PMMA, polyethylene, polypropylene, polyesters, epoxy resins; metal substrates and painted composites.
• compositions according to the invention once advantageously lead, after crosslinking, to an adhesive joint having semi-structural or structural properties.
• composition according to the invention advantageously results in an adhesive seal having a modulus at break greater than or equal to 20 MPa, and in particular greater than or equal to 25 MPa.
• compositions according to the invention advantageously exhibit, after crosslinking, good adhesive properties, while having a weak or even no odor.
• All of the embodiments described above can be combined with each other.
• the various aforementioned constituents of the composition, and in particular the preferred modes, of the composition can be combined with each other.
• by “between x and y”, or “ranging from x to y”, is meant an interval in which the limits x and y are included.
• the range “between 0% and 25%” notably includes the values 0% and 25%.
• HEMA 2-hydroxyethyl methacrylate
• PPG Polypropylene Glycol
• - AEROSIL ® R202 (CAS Number: 67762-90-7): a hydrophobic fumed silica (post-treated PDMS) with a specific surface area (BET) equal to 100 ⁇ 20 m 2 / g marketed by EVONIK;
• - VIKOFLEX® 7170 marketed by ARKEMA is an epoxidized soybean oil used as a plasticizer
• - CRAYVALLAC SLT marketed by ARKEMA is a micronized amide wax used as a rheological agent
• Voranol TM P2000 polyol was introduced and heated to 90 ° C under vacuum to dehydrate the polyol for about 1 hour.
• Desmodur 44 MC was introduced into the reactor and heated at 70 ° C for about 2 h. After a few minutes, the catalyst and 2-hydroxyethyl methacrylate were introduced, and the reaction medium was mixed at 60 ° C for 1 h.
• Component A and component B above were mixed, in a volume ratio of 10: 1.
• the mixing is carried out at a temperature of approximately 23 ° C., according to the volume ratio given with a static mixer.
• Comparative composition No. 2 was prepared in the same way with the following ingredients:
• Example 3 Results Measurement of tensile strength by tensile test:
• the resistance measurement (tensile stress) by tensile test was carried out according to the protocol described below.
• the principle of the measurement consists in stretching in a tensile machine, the movable jaw of which moves at a constant speed equal to 100 mm / minute, a standard specimen consisting of the crosslinked composition and recording, at the moment when the rupture occurs. of the test piece, the applied tensile stress (in MPa) as well as the elongation of the test piece (in%).
• the standard test piece is in the shape of a dumbbell, as illustrated in the international standard ISO 37 of 2011.
• the narrow part of the dumbbell used has a length of 20 mm, a width of 4 mm and a thickness of 500 Dm.
• the bondings are made on aluminum sterigmas from the Rocholl company. On a sterigma, an area of 25 * 12.5mm was delimited using Teflon wedges 250 ⁇ m thick, an area of 25 * 12.5mm. This zone was filled with the composition to be tested, then a second sterigma of the same material was laminated. The set was maintained by a clamp and placed in an air-conditioned room at 23 ° C or 100 ° C and 50% RH (relative humidity) for one week before traction on a dynamometer. The purpose of traction on a dynamometer is to evaluate the maximum force (in MPa) to be exerted on the assembly to separate it.
• a tensile machine makes it possible to subject a single lap joint placed between two rigid supports to a shear stress until failure by exerting a tension on the supports parallel to the surface of the assembly and to the principal axis of the test piece.
• the result to be recorded is the force or stress at break.
• the shear stress is applied via the movable jaw of the tensile machine with a displacement at the speed of 5 mm / min. This traction method is carried out as defined by the standard EN 1465 of 2009.
• Composition No. 1 advantageously leads to bonding to aluminum leading to a cohesive rupture (RC), which indicates in particular good adhesion in the automotive field compared to obtaining an adhesive rupture RA.
• the maximum force (Fmax) at the moment of rupture is advantageously higher with composition n ° 1 than that obtained with comparative composition n ° 2
• composition No. 1 advantageously results in an adhesive joint having, after crosslinking, a tensile strength greater than that obtained with composition No. 2 (comparative).

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Polyurethanes Or Polyureas (AREA)
• Macromonomer-Based Addition Polymer (AREA)
• Paints Or Removers (AREA)
• Adhesives Or Adhesive Processes (AREA)

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• 2019
  • 2019-03-28 FR FR1903224A patent/FR3094375B1/fr active Active
• 2020
  • 2020-03-25 US US17/442,698 patent/US20220119582A1/en active Pending
  • 2020-03-25 JP JP2021557495A patent/JP2022526355A/ja active Pending
  • 2020-03-25 EP EP20712377.9A patent/EP3947497A1/de active Pending
  • 2020-03-25 CN CN202080025913.2A patent/CN113631609B/zh active Active
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